@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP195689.RAgoDMvjT3nmjznbjhFkeJy1H73Qitgdd5YO3l09q-eek> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP195689.RAgoDMvjT3nmjznbjhFkeJy1H73Qitgdd5YO3l09q-eek130_head {
  this: np:hasAssertion dgn-np:NP195689.RAgoDMvjT3nmjznbjhFkeJy1H73Qitgdd5YO3l09q-eek130_assertion ;
    np:hasProvenance dgn-np:NP195689.RAgoDMvjT3nmjznbjhFkeJy1H73Qitgdd5YO3l09q-eek130_provenance ;
    np:hasPublicationInfo dgn-np:NP195689.RAgoDMvjT3nmjznbjhFkeJy1H73Qitgdd5YO3l09q-eek130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP195689.RAgoDMvjT3nmjznbjhFkeJy1H73Qitgdd5YO3l09q-eek130_assertion a np:Assertion .
  dgn-np:NP195689.RAgoDMvjT3nmjznbjhFkeJy1H73Qitgdd5YO3l09q-eek130_provenance a np:Provenance .
  dgn-np:NP195689.RAgoDMvjT3nmjznbjhFkeJy1H73Qitgdd5YO3l09q-eek130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP195689.RAgoDMvjT3nmjznbjhFkeJy1H73Qitgdd5YO3l09q-eek130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  lld:C0016667 a ncit:C7057 .
  dgn-gda:DGNd307c505ffed14e0e9609711602d9699 sio:SIO_000628 miriam-gene:3630 , lld:C0016667 ;
    a sio:SIO_001121 .
}
dgn-np:NP195689.RAgoDMvjT3nmjznbjhFkeJy1H73Qitgdd5YO3l09q-eek130_provenance {
  dgn-np:NP195689.RAgoDMvjT3nmjznbjhFkeJy1H73Qitgdd5YO3l09q-eek130_assertion dcterms:description "[They have been implicated in the regulation of developmental timing and pattern formation, restriction of differentiation potential, regulation of insulin secretion, resistance to viral infection, and in genomic rearrangements associated with carcinogenesis or other genetic disorders, such as fragile X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:17402793 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP195689.RAgoDMvjT3nmjznbjhFkeJy1H73Qitgdd5YO3l09q-eek130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:47+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}